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Arylation of Axially Chiral Phosphorothioate Salts by Dinuclear Pd(I) Catalysis
S‐aryl phosphorothioates are privileged motifs in pharmaceuticals, agrochemicals, and catalysts; yet, the challenge of devising a straightforward synthetic route to enantioenriched S‐aryl phosphorothioates has remained unsolved to date. We demonstrate herein the first direct C−SP(=O)(OR′)(OR′′) coup...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6771726/ https://www.ncbi.nlm.nih.gov/pubmed/31190467 http://dx.doi.org/10.1002/anie.201906063 |
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author | Chen, Xiang‐Yu Pu, Maoping Cheng, Hong‐Gang Sperger, Theresa Schoenebeck, Franziska |
author_facet | Chen, Xiang‐Yu Pu, Maoping Cheng, Hong‐Gang Sperger, Theresa Schoenebeck, Franziska |
author_sort | Chen, Xiang‐Yu |
collection | PubMed |
description | S‐aryl phosphorothioates are privileged motifs in pharmaceuticals, agrochemicals, and catalysts; yet, the challenge of devising a straightforward synthetic route to enantioenriched S‐aryl phosphorothioates has remained unsolved to date. We demonstrate herein the first direct C−SP(=O)(OR′)(OR′′) coupling of diverse and chiral phosphorothioate salts with aryl iodides, enabled by an air‐ and moisture‐stable Pd(I) dimer. Our mechanistic and computational data suggest distinct dinuclear Pd(I) catalysis to be operative, which allows for operationally simple couplings with broad scope and full retention of stereochemistry. |
format | Online Article Text |
id | pubmed-6771726 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-67717262019-10-07 Arylation of Axially Chiral Phosphorothioate Salts by Dinuclear Pd(I) Catalysis Chen, Xiang‐Yu Pu, Maoping Cheng, Hong‐Gang Sperger, Theresa Schoenebeck, Franziska Angew Chem Int Ed Engl Communications S‐aryl phosphorothioates are privileged motifs in pharmaceuticals, agrochemicals, and catalysts; yet, the challenge of devising a straightforward synthetic route to enantioenriched S‐aryl phosphorothioates has remained unsolved to date. We demonstrate herein the first direct C−SP(=O)(OR′)(OR′′) coupling of diverse and chiral phosphorothioate salts with aryl iodides, enabled by an air‐ and moisture‐stable Pd(I) dimer. Our mechanistic and computational data suggest distinct dinuclear Pd(I) catalysis to be operative, which allows for operationally simple couplings with broad scope and full retention of stereochemistry. John Wiley and Sons Inc. 2019-07-09 2019-08-12 /pmc/articles/PMC6771726/ /pubmed/31190467 http://dx.doi.org/10.1002/anie.201906063 Text en © 2019 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Communications Chen, Xiang‐Yu Pu, Maoping Cheng, Hong‐Gang Sperger, Theresa Schoenebeck, Franziska Arylation of Axially Chiral Phosphorothioate Salts by Dinuclear Pd(I) Catalysis |
title | Arylation of Axially Chiral Phosphorothioate Salts by Dinuclear Pd(I) Catalysis |
title_full | Arylation of Axially Chiral Phosphorothioate Salts by Dinuclear Pd(I) Catalysis |
title_fullStr | Arylation of Axially Chiral Phosphorothioate Salts by Dinuclear Pd(I) Catalysis |
title_full_unstemmed | Arylation of Axially Chiral Phosphorothioate Salts by Dinuclear Pd(I) Catalysis |
title_short | Arylation of Axially Chiral Phosphorothioate Salts by Dinuclear Pd(I) Catalysis |
title_sort | arylation of axially chiral phosphorothioate salts by dinuclear pd(i) catalysis |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6771726/ https://www.ncbi.nlm.nih.gov/pubmed/31190467 http://dx.doi.org/10.1002/anie.201906063 |
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